Simultaneous manipulation and imaging of chemogenetically induced hydrogen peroxide in hardly transfectable endothelial cells

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dc.authorid0000-0002-9373-0808
dc.contributor.authorEroğlu, Emrah
dc.date.accessioned2023-08-16T10:49:09Z
dc.date.available2023-08-16T10:49:09Z
dc.date.issued2022
dc.departmentİstanbul Medipol Üniversitesi, Rektörlük, Sağlık Bilim ve Teknolojileri Araştırma Enstitüsü
dc.description.abstractHydrogen peroxide (H2O2) is a critical signaling molecule in vascular cells, which controls signaling events, yet it can cause pathological oxidative stress in excess. The lack of suitable tools undermined experimental approaches to study the role of oxidative eu- and distress in cellular ultra-locales. This study exploits a yeast-derived D-amino acid oxidase (mDAAO) as a chemogenetic tool to induce, visualize and test the cytotoxicity of H2O2 in hardly transfectable endothelial cells. Due to the poor transfectability of endothelial cells, lentiviral vectors have been used to generate cell lines stably expressing mDAAOs. mDAAOs are substrate-based chemogenetic enzymes that convert D-amino acids to their corresponding alpha-keto acids and generate H2O2 as a byproduct, which can be visualized with a novel ultrasensitive, and ratiometric H2O2 biosensor termed HyPer7. This study tested the suitability of two different D-amino acids, including D-alanine and D-methionine, to induce oxidative stress in endothelial cells. Live-cell imaging experiments unveiled that 10 mM D-methionine generated significantly higher and faster H2O2 signals than D-alanine. However, both D-amino acids induced comparable levels of cell death documented by a colorimetric cell metabolic activity assay (MTT). This study provides a guide for manipulating and monitoring the cytotoxic effect of H2O2 in endothelial cells.
dc.identifier.citationEroğlu, E. (2022). Simultaneous manipulation and imaging of chemogenetically induced hydrogen peroxide in hardly transfectable endothelial cells. Cumhuriyet Science Journal, 43(4), 645-651. https://dx.doi.org/10.17776/csj.1114125
dc.identifier.doi10.17776/csj.1114125
dc.identifier.endpage651
dc.identifier.issn2587-2680
dc.identifier.issn2587-246X
dc.identifier.issue4
dc.identifier.startpage645
dc.identifier.trdizinid1149869
dc.identifier.urihttps://dx.doi.org/10.17776/csj.1114125
dc.identifier.urihttps://hdl.handle.net/20.500.12511/11335
dc.identifier.volume43
dc.indekslendigikaynakTR-Dizin
dc.institutionauthorEroğlu, Emrah
dc.language.isoen
dc.publisherSivas Cumhuriyet University
dc.relation.ispartofCumhuriyet Science Journalen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectChemogenetic Tools
dc.subjectEndothelial Cells
dc.subjectHydrogen Peroxide
dc.subjectGenetically Encoded Biosensors
dc.subjectCytotoxicity
dc.titleSimultaneous manipulation and imaging of chemogenetically induced hydrogen peroxide in hardly transfectable endothelial cells
dc.typeArticle

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